Canonical Allele Identifier: CA413143637

Gene: HUWE1

Linked Data

• MyVariant Identifiers: chrX:g.53560989C>G (hg19) ; chrX:g.53534028C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.53534028C>G , CM000685.2:g.53534028C>G	GRCh38
NC_000023.10:g.53560989C>G , CM000685.1:g.53560989C>G	GRCh37
NC_000023.9:g.53577714C>G	NCBI36
NG_016261.2:g.157706G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704099.1:c.12785G>C	ENSP00000515693.1:p.Arg4262Pro
ENST00000262854.11:c.13001G>C MANE Select	ENSP00000262854.6:p.Arg4334Pro
ENST00000262854.10:c.13001G>C	ENSP00000262854.6:p.Arg4334Pro
ENST00000342160.7:c.13001G>C	ENSP00000340648.3:p.Arg4334Pro
ENST00000426907.5:c.3468G>C
ENST00000488459.1:n.314G>C
ENST00000612484.4:c.12974G>C	ENSP00000479451.1:p.Arg4325Pro
NM_031407.6:c.13001G>C	NP_113584.3:p.Arg4334Pro
XM_005261965.2:c.13001G>C	XP_005262022.1:p.Arg4334Pro
XM_011530746.1:c.13250G>C	XP_011529048.1:p.Arg4417Pro
XM_011530747.1:c.13250G>C	XP_011529049.1:p.Arg4417Pro
XM_011530748.1:c.13250G>C	XP_011529050.1:p.Arg4417Pro
XM_011530749.1:c.13250G>C	XP_011529051.1:p.Arg4417Pro
XM_011530750.1:c.13250G>C	XP_011529052.1:p.Arg4417Pro
XM_011530751.1:c.13250G>C	XP_011529053.1:p.Arg4417Pro
XM_011530752.1:c.13247G>C	XP_011529054.1:p.Arg4416Pro
XM_011530753.1:c.13205G>C	XP_011529055.1:p.Arg4402Pro
XM_011530754.1:c.13202G>C	XP_011529056.1:p.Arg4401Pro
XM_011530755.1:c.13199G>C	XP_011529057.1:p.Arg4400Pro
XM_011530756.1:c.13151G>C	XP_011529058.1:p.Arg4384Pro
XM_011530757.1:c.12848G>C	XP_011529059.1:p.Arg4283Pro
XM_005261965.4:c.13001G>C	XP_005262022.1:p.Arg4334Pro
XM_011530751.2:c.13250G>C	XP_011529053.1:p.Arg4417Pro
XM_017029191.1:c.13382G>C	XP_016884680.1:p.Arg4461Pro
XM_017029192.1:c.13379G>C	XP_016884681.1:p.Arg4460Pro
XM_017029193.1:c.13361G>C	XP_016884682.1:p.Arg4454Pro
XM_017029194.1:c.13337G>C	XP_016884683.1:p.Arg4446Pro
XM_017029195.1:c.13334G>C	XP_016884684.1:p.Arg4445Pro
XM_017029196.1:c.13331G>C	XP_016884685.1:p.Arg4444Pro
XM_017029197.1:c.13283G>C	XP_016884686.1:p.Arg4428Pro
XM_017029198.2:c.13271G>C	XP_016884687.1:p.Arg4424Pro
XM_017029199.1:c.13271G>C	XP_016884688.1:p.Arg4424Pro
XM_017029200.1:c.13271G>C	XP_016884689.1:p.Arg4424Pro
XM_017029201.1:c.13271G>C	XP_016884690.1:p.Arg4424Pro
XM_017029202.1:c.13271G>C	XP_016884691.1:p.Arg4424Pro
XM_017029203.1:c.13271G>C	XP_016884692.1:p.Arg4424Pro
XM_017029204.1:c.13133G>C	XP_016884693.1:p.Arg4378Pro
XM_017029206.1:c.12980G>C	XP_016884695.1:p.Arg4327Pro
XM_024452322.1:c.13250G>C	XP_024308090.1:p.Arg4417Pro
NM_031407.7:c.13001G>C MANE Select	NP_113584.3:p.Arg4334Pro